A Study to Assess the Long-Term Safety and Efficacy of Donidalorsen in the Prophylactic Treatment of Hereditary Angioedema (HAE)

  • STATUS
    Recruiting
  • End date
    Mar 20, 2027
  • participants needed
    144
  • sponsor
    Ionis Pharmaceuticals, Inc.
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Updated on 20 August 2023
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angioedema

Summary

The purpose of this study is to evaluate the long-term safety and efficacy of donidalorsen in people with HAE and the effects of donidalorsen on the number of HAE attacks and their impact on quality of life (QoL).

Description

This is a Phase 3, multi-center, open-label, global study with donidalorsen in up to approximately 144 participants with HAE-1 (Type I) and HAE-2 (Type II). There are two groups in this study: 1) participants who roll over from another study of donidalorsen (open-label extension [OLE] participants), and 2) new participants who are not rolling over from another study of donidalorsen and were previously maintained on HAE prophylactic therapy with lanadelumab, berotralstat, or a C1-esterase inhibitor (C1-INH). The length of participation in the study is approximately 70 weeks for OLE participants and 76 weeks for other participants. Participants will receive donidalorsen in an Extended Treatment Period for up to an additional 104 weeks.

Details
Condition Hereditary Angioedema
Treatment donidalorsen
Clinical Study IdentifierNCT05392114
SponsorIonis Pharmaceuticals, Inc.
Last Modified on20 August 2023

Eligibility

 Yes No Not Sure

Inclusion Criteria

Participants and, as applicable, legally authorized representatives (i.e., parent(s)/legal guardian), must provide written and signed informed consent form (ICF)
Participants must have access to, and the ability to use, ≥ 1 acute medication(s) (e.g., plasma-derived or recombinant C1-INH concentrate or a bradykinin receptor (BK) 2-receptor antagonist) to treat angioedema attacks
Open-Label Extension Participants ONLY
Participants must be aged ≥ 12 years at the time of informed consent and, as applicable, assent
Satisfactory completion of ISIS 721744-CS5 (randomized placebo-controlled index study) through Week 25 or participants who are allowed to exit ISIS 721744-CS5 study per protocol with an acceptable safety and tolerability profile
Participants must have a documented diagnosis of HAE-1/HAE-2
New (not previously on donidalorsen) Participants ONLY
Participants must be on a stable dose (≥ 12 weeks) of prophylaxis treatment with lanadelumab or berotralstat or SC C1-esterase inhibitor prior to the Screening Period

Exclusion Criteria

Open-Label Extension Participants
Concurrent diagnosis of any other type of recurrent angioedema, including acquired, idiopathic angioedema or HAE with normal C1-INH (also known as HAE Type III)
Anticipated change in the use of concurrent androgen or tranexamic acid prophylaxis used to prevent angioedema attacks
Any clinically-significant abnormalities in screening laboratory values
Have any new condition or worsening of an existing condition or change or anticipated change in medication
New (not previously on donidalorsen) Participants ONLY
Malignancy within 5 years of Screening, except for non-melanoma skin cancers, cervical in situ carcinoma, breast ductal carcinoma in situ, or stage 1 prostate carcinoma that has been successfully treated
Hypersensitivity to the active substance (donidalorsen) or to any of the excipients
Treatment with another investigational drug (non-oligonucleotide) or biological agent within 1 month of Screening or 5 half-lives of investigational agent, whichever is longer
Recent history of, or current drug or alcohol abuse
Participated in a prior donidalorsen study
Exposure to any of the following medications
Angiotensin-converting enzyme (ACE) inhibitors or any estrogen containing medications with systemic absorption
Oligonucleotides (including small interfering ribonucleic acid [siRNA]) within 4 months of Screening if single dose received, or within 12 months of Screening if multiple doses received. This exclusion does not apply to vaccines
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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